D59G (p.Asp59Gly) variant of FLG (Filaggrin)
D59G (p.Asp59Gly) in FLG (Filaggrin) is a missense change. The record also includes variant effect predictions and population frequency data.
D59G (p.Asp59Gly) variant details
- p.Asp59Gly
- gnomAD rs1385160385
- Missense
- REVEL 0.22
- CADD 24.30
- PolyPhen-2 0.72
- SIFT 0.68
- Most common in the Non-Finnish European population (allele frequency 9e-07)